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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 321893Generated: October 30, 2026

Hydrochloric Acid → HCID 22007973, compound

https://huagongshe.com/reaction/321893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantHCID 13609014HCID 13609014—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22007973HCID 2200797367.9%

Reaction Conditions

Temperature-60 °C

Reaction Steps

In a mixture of 48.9 g (248.8 imol) of (4-propylphenyl)acetylchloride, 2.6 g (7.5 mmol) of tris(2,4-pentanedionata)iron (III), and 200 ml of toluene was added dropwise a solution of a Grignard reagent prepared from 56.6 g (323.5 mmol) of 1-bromo-3-fluorobenzene and 8.2 g (335.9 mmol) of Mg in 300 ml of tetrahydrofuran (THF) while maintaining them at a temperature lower than −60° C. After finishing of the dropping, they were stirred at the same temperature for 3 hours. Subsequently, the reaction mixture was raised up to room temperature, 200 ml of a diluted hydrochloric acid was added dropwise thereto, and then extracted with 150 ml of heptane. The organic layer thus obtained was washed with an aqueous sodium bicarbonate solution thrice and with water thrice, and then dried over anhydrous magnesium sulfate. After the solvent was distilled off under a reduced pressure, the residue was subjected to silica gel column chromatography (eluent: toluene/heptane=8/2) to obtain 43.3 g of a crude 3-fluoro-4′-propyldeoxybenzoin. This product was recrystallized from methanol to obtain 28.5 g of the subject compound. (Yield: 44.8%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06210603B1
Source datasetuspto-grants-2001_04
ORD IDord-dc8078d69dbc4434a2ff1900e45352b0
Source noteuspto-grants-2001_04